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1. GDP Audit Checklist
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2. Quality Agreement
Standard draft to adapt and extend

 

3. Premises
Official requirements | material flow | room classes | and much more...

 

4. GMP Audit Checklist
for Pharmaceutical and API Manufacturers

 

5. Documenting Process Validation
A Drugmaker‘s Guide – step-by-step manual based on real-world examination experience

 

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News about GMP/cGMP

Maas & Peither at PDA/EMEA Conference

Today the PDA/EMEA Joint Conference starts in Berlin, Germany. Maas & Peither is present at booth #18 at this important European Conference.

 

Maas & Peither is presenting the GMP MANUAL the GMP knowledge source out of the practice for the pharmaceutical industry. The GMP MANUAL got a lot of attention at the recent PDA/FDA Conference in Washington. The knowledge source is used by approx. 10.000 professionals around the world.

We will report about important developments after the conference.

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